Status:

COMPLETED

Combination Antibiotic Treatment for Reactive Arthritis Caused by Chlamydia Bacteria

Lead Sponsor:

University of South Florida

Collaborating Sponsors:

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Conditions:

Arthritis, Reactive

Reiter Disease

Eligibility:

All Genders

18-70 years

Phase:

PHASE3

Brief Summary

Reactive arthritis, also known as Reiter's syndrome, is a form of arthritis that occurs as a reaction to an infection elsewhere in the body. It is characterized by inflammation of the joints, tendons,...

Detailed Description

The initial infection that causes reactive arthritis is caused by one of two bacteria: Chlamydia trachomatis, which is usually acquired through sexual contact, or Chlamydia pneumoniae, which can cause...

Eligibility Criteria

Inclusion

  • Meet the following European Spondyloarthropathy Study Group Criteria:
  • inflammatory spinal pain OR
  • synovitis AND
  • one or more of the following:
  • positive family history
  • urethritis or cervicitis within 1 month prior to onset of arthritis
  • buttock pain
  • enthesopathy
  • sacroiliitis
  • Disease duration of at least 6 months
  • Negative pregnancy test at study baseline and willing to use an effective method of contraception other than combined oral contraceptives for the duration of the study (for women of childbearing age)

Exclusion

  • Sensitivity or history of allergic reaction to rifampin, doxycycline, or azithromycin
  • Currently taking any medications that may interact with the study medications, specifically rifampin
  • Liver transaminases greater than or equal to two times the normal level
  • Significant abnormalities in the complete blood count (CBC)
  • Pregnant
  • Current psoriasis
  • Diagnosis of inflammatory bowel disease
  • Diagnosis of ankylosing spondylitis
  • Previous prolonged exposure to antibiotics (more than 2 weeks) as a potential treatment for reactive arthritis

Key Trial Info

Start Date :

May 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2008

Estimated Enrollment :

42 Patients enrolled

Trial Details

Trial ID

NCT00351273

Start Date

May 1 2006

End Date

September 1 2008

Last Update

November 13 2018

Active Locations (3)

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Page 1 of 1 (3 locations)

1

University of South Florida

Tampa, Florida, United States, 33612

2

Louisiana State University

New Orleans, Louisiana, United States, 70112

3

University of Toronto

Toronto, Ontario, Canada, M5T 2S8